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FDA 510(k)

CAPILLARY PERFUSION MONITOR #LD5000

K-Number: K812005 · 1982-02-04

ApplicantNuclear Pacific, Inc.
Decision Date1982-02-04
Product CodeDPW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CAPILLARY PERFUSION MONITOR #LD5000 is the device name listed in this FDA 510(k) record. The listed applicant is Nuclear Pacific, Inc.. It received FDA 510(k) clearance on 1982-02-04 under 510(k) number K812005. The device is classified under product code DPW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAPILLARY PERFUSION MONITOR #LD5000?

CAPILLARY PERFUSION MONITOR #LD5000 is a medical device that received FDA 510(k) clearance on 1982-02-04. The listed applicant is Nuclear Pacific, Inc.. The 510(k) number is K812005.

When did CAPILLARY PERFUSION MONITOR #LD5000 receive FDA 510(k) clearance?

CAPILLARY PERFUSION MONITOR #LD5000 received FDA 510(k) clearance on 1982-02-04, under 510(k) number K812005.

Who is the listed applicant for CAPILLARY PERFUSION MONITOR #LD5000?

The FDA 510(k) record lists Nuclear Pacific, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CAPILLARY PERFUSION MONITOR #LD5000?

The FDA product code for CAPILLARY PERFUSION MONITOR #LD5000 is DPW.

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Related Devices (Code: DPW)

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Official Source

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